Canonical Allele Identifier: CA351496838

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626435T>A (hg19) ; chr3:g.12584936T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584936T>A , CM000665.2:g.12584936T>A	GRCh38
NC_000003.11:g.12626435T>A , CM000665.1:g.12626435T>A	GRCh37
NC_000003.10:g.12601435T>A	NCBI36
NG_007467.1:g.84244A>T , LRG_413:g.84244A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1379A>T (RAF1)	ENSP00000401088.1:n.*1379A>T
ENST00000432427.3:c.1031A>T (RAF1)
ENST00000460610.2:n.6026A>T (RAF1)
ENST00000471449.2:n.524A>T (RAF1)
ENST00000475353.2:n.3994A>T (RAF1)
ENST00000684903.1:c.*1391A>T (RAF1)	ENSP00000508612.1:n.*1391A>T
ENST00000685348.1:c.*1425A>T (RAF1)	ENSP00000510285.1:n.*1425A>T
ENST00000685437.1:c.1615A>T (RAF1)	ENSP00000508794.1:p.Lys539Ter
ENST00000685653.1:c.1714A>T (RAF1)	ENSP00000509968.1:p.Lys572Ter
ENST00000685697.1:n.2449A>T (RAF1)
ENST00000685738.1:c.*678A>T (RAF1)	ENSP00000510156.1:n.*678A>T
ENST00000686409.1:n.5123A>T (RAF1)
ENST00000686455.1:n.4435A>T (RAF1)
ENST00000686762.1:c.*273A>T (RAF1)	ENSP00000509767.1:n.*273A>T
ENST00000687257.1:n.4168A>T (RAF1)
ENST00000687326.1:c.*3006A>T (RAF1)	ENSP00000509665.1:n.*3006A>T
ENST00000687505.1:n.1832A>T (RAF1)
ENST00000687923.1:c.1603A>T (RAF1)	ENSP00000510255.1:p.Lys535Ter
ENST00000688269.1:n.2310A>T (RAF1)
ENST00000688444.1:n.3831A>T (RAF1)
ENST00000688543.1:c.1615A>T (RAF1)	ENSP00000509612.1:p.Lys539Ter
ENST00000688625.1:c.*3083A>T (RAF1)	ENSP00000509522.1:n.*3083A>T
ENST00000688803.1:n.3142A>T (RAF1)
ENST00000688914.1:n.1127A>T (RAF1)
ENST00000689097.1:c.*1391A>T (RAF1)	ENSP00000509756.1:n.*1391A>T
ENST00000689389.1:c.1537A>T (RAF1)	ENSP00000510213.1:p.Lys513Ter
ENST00000689418.1:c.*3609A>T (RAF1)	ENSP00000509467.1:n.*3609A>T
ENST00000689540.1:n.4082A>T (RAF1)
ENST00000689876.1:c.*263A>T (RAF1)	ENSP00000508535.1:n.*263A>T
ENST00000689914.1:c.*648A>T (RAF1)	ENSP00000509847.1:n.*648A>T
ENST00000690397.1:c.1603A>T (RAF1)	ENSP00000508730.1:p.Lys535Ter
ENST00000690460.1:c.1702A>T (RAF1)	ENSP00000509106.1:p.Lys568Ter
ENST00000690585.1:c.440A>T (RAF1)
ENST00000690625.1:n.2750A>T (RAF1)
ENST00000691396.1:c.*1586A>T (RAF1)	ENSP00000510712.1:n.*1586A>T
ENST00000691643.1:n.2767A>T (RAF1)
ENST00000691724.1:c.*671A>T (RAF1)	ENSP00000509255.1:n.*671A>T
ENST00000691779.1:c.*1292A>T (RAF1)	ENSP00000508592.1:n.*1292A>T
ENST00000691888.1:c.588A>T (RAF1)
ENST00000691899.1:c.1714A>T (RAF1)	ENSP00000508763.1:p.Lys572Ter
ENST00000692069.1:n.4638A>T (RAF1)
ENST00000692093.1:c.1615A>T (RAF1)	ENSP00000509669.1:p.Lys539Ter
ENST00000692311.1:n.2538A>T (RAF1)
ENST00000692558.1:n.4297A>T (RAF1)
ENST00000692773.1:c.*1451A>T (RAF1)	ENSP00000509055.1:n.*1451A>T
ENST00000692830.1:c.*1459A>T (RAF1)	ENSP00000509461.1:n.*1459A>T
ENST00000693312.1:c.1489A>T (RAF1)	ENSP00000508686.1:p.Lys497Ter
ENST00000693664.1:c.*165A>T (RAF1)	ENSP00000509614.1:n.*165A>T
ENST00000693705.1:c.*1093A>T (RAF1)	ENSP00000510697.1:n.*1093A>T
ENST00000251849.9:c.1714A>T (RAF1) MANE Select	ENSP00000251849.4:p.Lys572Ter
ENST00000442415.7:c.1774A>T (RAF1)	ENSP00000401888.2:p.Lys592Ter
ENST00000676541.1:c.*2683T>A (MKRN2)	ENSP00000503730.1:n.*2683T>A
ENST00000677142.1:c.*2683T>A (MKRN2)	ENSP00000504455.1:n.*2683T>A
ENST00000677816.1:c.*1238T>A (MKRN2)	ENSP00000502893.1:n.*1238T>A
ENST00000677941.1:n.2746T>A (MKRN2)
ENST00000251849.8:c.1714A>T (RAF1)	ENSP00000251849.4:p.Lys572Ter
ENST00000423275.5:c.*1391A>T (RAF1)	ENSP00000401088.1:n.*1391A>T
ENST00000432427.2:c.1351A>T (RAF1)	ENSP00000398591.2:p.Lys451Ter
ENST00000442415.6:c.1774A>T (RAF1)	ENSP00000401888.2:p.Lys592Ter
ENST00000471449.1:n.403A>T (RAF1)
NM_002880.3:c.1714A>T , LRG_413t1:c.1714A>T (RAF1)	NP_002871.1:p.Lys572Ter
XM_005265355.1:c.1714A>T (RAF1)	XP_005265412.1:p.Lys572Ter
XM_005265357.1:c.1615A>T (RAF1)	XP_005265414.1:p.Lys539Ter
XM_005265358.3:c.1471A>T (RAF1)	XP_005265415.1:p.Lys491Ter
XM_005265359.3:c.1372A>T (RAF1)	XP_005265416.1:p.Lys458Ter
XM_011533974.1:c.1714A>T (RAF1)	XP_011532276.1:p.Lys572Ter
XM_011533975.1:c.1471A>T (RAF1)	XP_011532277.1:p.Lys491Ter
NM_001354689.1:c.1774A>T (RAF1)	NP_001341618.1:p.Lys592Ter
NM_001354690.1:c.1714A>T (RAF1)	NP_001341619.1:p.Lys572Ter
NM_001354691.1:c.1471A>T (RAF1)	NP_001341620.1:p.Lys491Ter
NM_001354692.1:c.1471A>T (RAF1)	NP_001341621.1:p.Lys491Ter
NM_001354693.1:c.1615A>T (RAF1)	NP_001341622.1:p.Lys539Ter
NM_001354694.1:c.1531A>T (RAF1)	NP_001341623.1:p.Lys511Ter
NM_001354695.1:c.1372A>T (RAF1)	NP_001341624.1:p.Lys458Ter
NR_148940.1:n.2242A>T (RAF1)
NR_148941.1:n.2188A>T (RAF1)
NR_148942.1:n.2127A>T (RAF1)
XM_011533974.3:c.1714A>T (RAF1)	XP_011532276.1:p.Lys572Ter
XM_017006966.1:c.1615A>T (RAF1)	XP_016862455.1:p.Lys539Ter
NM_001354689.3:c.1774A>T (RAF1)	NP_001341618.1:p.Lys592Ter
NM_001354690.2:c.1714A>T (RAF1)	NP_001341619.1:p.Lys572Ter
NM_001354691.2:c.1471A>T (RAF1)	NP_001341620.1:p.Lys491Ter
NM_001354692.2:c.1471A>T (RAF1)	NP_001341621.1:p.Lys491Ter
NM_001354693.2:c.1615A>T (RAF1)	NP_001341622.1:p.Lys539Ter
NM_001354694.2:c.1531A>T (RAF1)	NP_001341623.1:p.Lys511Ter
NM_001354695.2:c.1372A>T (RAF1)	NP_001341624.1:p.Lys458Ter
NR_148940.2:n.2158A>T (RAF1)
NR_148941.2:n.2104A>T (RAF1)
NR_148942.2:n.2043A>T (RAF1)
NM_001354690.3:c.1714A>T (RAF1)	NP_001341619.1:p.Lys572Ter
NM_001354691.3:c.1471A>T (RAF1)	NP_001341620.1:p.Lys491Ter
NM_001354692.3:c.1471A>T (RAF1)	NP_001341621.1:p.Lys491Ter
NM_001354693.3:c.1615A>T (RAF1)	NP_001341622.1:p.Lys539Ter
NM_001354694.3:c.1531A>T (RAF1)	NP_001341623.1:p.Lys511Ter
NM_001354695.3:c.1372A>T (RAF1)	NP_001341624.1:p.Lys458Ter
NM_002880.4:c.1714A>T (RAF1) MANE Select	NP_002871.1:p.Lys572Ter
NR_148940.3:n.2158A>T (RAF1)
NR_148941.3:n.2104A>T (RAF1)
NR_148942.3:n.2043A>T (RAF1)